Annotation Detail for CRYGN

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Basic Information Top

Gene Symbol:	CRYGN ( MGC119042,MGC119043,MGC119044,MGC119045 )
Gene Full Name:	crystallin, gamma N
Band:	7q36.1
Quick Links	Entrez ID:155051; OMIM: 609603; Uniprot ID:CRGN_HUMAN; ENSEMBL ID: ENSG00000127377; HGNC ID: 20458
Relate to Another Database:	SFARIGene; denovo-db

Pathways, Diseases and Drugs

TF binding site

Post Translation Modification

Validated transcription factor binding site by ChIP-Chip and ChIP-Seq

RefSeq ID: NM_144727
Location:chr7 150757989-150768031
strand:-

Upstream the gene:12 results
Downstream the gene:3 results
Inside the gene:5 results

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	CD4	GSE12889	150776785	150776959	174	8841
CTCF	CD4	SISSRdata	150776785	150776959	174	8841
CTCF	G2	GSE9613	150768242	150769036	794	608
CTCF	G2	GSE9613	150776465	150776902	437	8652
CTCF	G2	GSE9613	150779275	150779436	161	11324
Myc	hES	GSE17917	150776239	150776506	267	8341
NRSF	mAb	Jurkat	150779275	150779436	161	11324
Stat6	IL-4-hr1	GSE17850	150769243	150769935	692	1558
TFAP2C	MCF7	GSE21234	150776508	150777067	559	8756
hScc1	Bcell	GSE12603	150768125	150768804	679	433
hScc1	Bcell	GSE12603	150776215	150776902	687	8527
hScc1	CdLS	GSE12603	150776143	150776902	759	8491

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	G2	GSE9613	150755183	150755827	644	2485
RARA	MCF7	GSE15244	150756062	150757103	1041	1407
hScc1	Bcell	GSE12603	150757775	150757954	179	125

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	G2	GSE9613	150758807	150759013	206	0
CTCF	G2	GSE9613	150759467	150759764	297	0
CTCF	G2	GSE9613	150760326	150761027	701	0
CTCF	G2	GSE9613	150764774	150765522	748	0
H3K27me3	colorectal	cancer	150766816	150767344	528	0

Validated miRNA targets

Cis-Nats regulation

Simple Query:

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

Studies: 1,036
Genes: 1,379
CNVs/SVs: 5,420
SNVs/Indels: 11,669
de novo Mutations: 5,669
Mosaics: 789
Linkage Regions: 172

Paper Collected: 6/30/2018

Last Update: 8/26/2018

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